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      Coupling between Voltage Sensors and Activation Gate in Voltage-gated K + Channels

      research-article
      , ,
      The Journal of General Physiology
      The Rockefeller University Press
      Shaker, DRK1, KcsA, S4-S5 linker, S6

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          Abstract

          Current through voltage-gated K + channels underlies the action potential encoding the electrical signal in excitable cells. The four subunits of a voltage-gated K + channel each have six transmembrane segments (S1–S6), whereas some other K + channels, such as eukaryotic inward rectifier K + channels and the prokaryotic KcsA channel, have only two transmembrane segments (M1 and M2). A voltage-gated K + channel is formed by an ion-pore module (S5–S6, equivalent to M1–M2) and the surrounding voltage-sensing modules. The S4 segments are the primary voltage sensors while the intracellular activation gate is located near the COOH-terminal end of S6, although the coupling mechanism between them remains unknown. In the present study, we found that two short, complementary sequences in voltage-gated K + channels are essential for coupling the voltage sensors to the intracellular activation gate. One sequence is the so called S4–S5 linker distal to the voltage-sensing S4, while the other is around the COOH-terminal end of S6, a region containing the actual gate-forming residues.

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          Crystal structure and mechanism of a calcium-gated potassium channel.

          Ion channels exhibit two essential biophysical properties; that is, selective ion conduction, and the ability to gate-open in response to an appropriate stimulus. Two general categories of ion channel gating are defined by the initiating stimulus: ligand binding (neurotransmitter- or second-messenger-gated channels) or membrane voltage (voltage-gated channels). Here we present the structural basis of ligand gating in a K(+) channel that opens in response to intracellular Ca(2+). We have cloned, expressed, analysed electrical properties, and determined the crystal structure of a K(+) channel (MthK) from Methanobacterium thermoautotrophicum in the Ca(2+)-bound, opened state. Eight RCK domains (regulators of K(+) conductance) form a gating ring at the intracellular membrane surface. The gating ring uses the free energy of Ca(2+) binding in a simple manner to perform mechanical work to open the pore.
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            Contribution of the S4 segment to gating charge in the Shaker K+ channel.

            Voltage-activated ion channels respond to changes in membrane voltage by coupling the movement of charges to channel opening. A K+ channel-specific radioligand was designed and used to determine the origin of these gating charges in the Shaker K+ channel. Opening of a Shaker K+ channel is associated with a displacement of 13.6 electron charge units. Gating charge contributions were determined for six of the seven positive charges in the S4 segment, an unusual amino acid sequence in voltage-activated cation channels consisting of repeating basic residues at every third position. Charge-neutralizing mutations of the first four positive charges led to large decreases (approximately 4 electron charge units each) in the gating charge; however, the gating charge of Shaker delta 10, a Shaker K+ channel with 10 altered nonbasic residues in its S4 segment, was found to be identical to the wild-type channel. These findings show that movement of the NH2-terminal half but not the CO2H-terminal end of the S4 segment underlies gating charge, and that this portion of the S4 segment appears to move across the entire transmembrane voltage difference in association with channel activation.
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              Voltage-sensing residues in the S2 and S4 segments of the Shaker K+ channel.

              The activation of Shaker K+ channels is steeply voltage dependent. To determine whether conserved charged amino acids in putative transmembrane segments S2, S3, and S4 contribute to the gating charge of the channel, the total gating charge movement per channel was measured in channels containing neutralization mutations. Of eight residues tested, four contributed significantly to the gating charge: E293, an acidic residue in S2, and R365, R368, and R371, three basic residues in the S4 segment. The results indicate that these residues are a major component of the voltage sensor. Furthermore, the S4 segment is not solely responsible for gating charge movement in Shaker K+ channels.
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                Author and article information

                Journal
                J Gen Physiol
                The Journal of General Physiology
                The Rockefeller University Press
                0022-1295
                1540-7748
                November 2002
                : 120
                : 5
                : 663-676
                Affiliations
                Department of Physiology, University of Pennsylvania, Philadelphia, PA 19104
                Author notes

                Address correspondence to Dr. Zhe Lu, University of Pennsylvania, Department of Physiology, D302A Richards Building, 3700 Hamilton Walk, Philadelphia, PA 19104. Fax: (215) 573-1940; E-mail: zhelu@ 123456mail.med.upenn.edu

                Article
                20028696
                10.1085/jgp.20028696
                2229552
                12407078
                1999f306-7fa2-4a48-a47d-beebac5c57ce
                Copyright © 2002, The Rockefeller University Press
                History
                : 9 August 2002
                : 24 September 2002
                : 25 September 2002
                Categories
                Article

                Anatomy & Physiology
                shaker,drk1,s4-s5 linker,kcsa,s6
                Anatomy & Physiology
                shaker, drk1, s4-s5 linker, kcsa, s6

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